Chapter 9 Discovery of the Double Helix

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35 Terms

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Who was the main founder of the alpha helix structure

According to Dr. V:

The main founder was Rosalind Franklin

<p>According to Dr. V: </p><p>The main founder was Rosalind Franklin </p>
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Rosalind Franklin and Maurice Wilkins

scientist who generated x-ray diffraction and crystallizing DNA

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DISCOVERIES:

- they discovered that DNA was double stranded

- discovered the actual distance of the base pairs from the sugars within a DNA strand based upon the x-ray diffraction experiment

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Rosalind Franklin (conclusion)

the diffraction pattern from her experiments suggested several structural features of DNA were:

- helical

- more than one strand

- 10 base pairs per complete turn

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James Watson and Francis Crick

Scientists who discovered the structure of DNA

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According to Dr. V they both stole the idea from Rosalind Franklin and got all the credit.

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Linus Pauling

proposed that regions of protein can fold into a secondary structure (alpha-helix)

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- was discovered in a similar scenario as Rosalind Franklin by using x-ray diffraction but this time studying the wet fibers of DNA

<p>proposed that regions of protein can fold into a secondary structure (alpha-helix) </p><p>--------------------------------</p><p>- was discovered in a similar scenario as Rosalind Franklin by using x-ray diffraction but this time studying the wet fibers of DNA</p>
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Erwin Chargaff (Chargaff's Rule)

discovered that A=T and G=C by analyzing base composition of DNA isolated from many different species

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DISCOVERY:

- based of his data he came to the conclusion that the ratios between complementaries are the same between A-T and C-G

<p>discovered that A=T and G=C by analyzing base composition of DNA isolated from many different species</p><p>--------------------------------</p><p>DISCOVERY:</p><p>- based of his data he came to the conclusion that the ratios between complementaries are the same between A-T and C-G</p>
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Erwin Chargaff (experiment)

1. For each type of cell chromosomal material was extracted either by using, high salt, detergent, or mild alkali treatment

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2. Removal of protein

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3. Hydrolyze the DNA to release the bases from the DNA strands

- treated genomic DNA with strong acid (to break convalent bonds between sugars and bases)

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Basic rule of thumb for Cargaff's rule

- Each base pair ALWAYS has 3 rings (purine + pyrimidine)

- the distance between A=T to G=C is always 3.4 nm

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B-form DNA

- 10 base pairs per turn

- 3.4 nm per turn

- the two strands are antiparallel

- is the most common structure

- is almost always has a 90-degree angle

- dsDNA (double-stranded)

- right-handed alpha-helix

- has a deep indentation called a "Major and Minor Groove"

<p>- 10 base pairs per turn </p><p>- 3.4 nm per turn </p><p>- the two strands are antiparallel</p><p>- is the most common structure</p><p>- is almost always has a 90-degree angle </p><p>- dsDNA (double-stranded) </p><p>- right-handed alpha-helix</p><p>- has a deep indentation called a "Major and Minor Groove"</p>
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antiparallel strands

Strands parallel to each other going in opposite directions

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- 3'-5' and 5'-3'

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HINT: legit just think the opposite of

<p>Strands parallel to each other going in opposite directions</p><p>--------------------------------</p><p>- 3'-5' and 5'-3'</p><p>--------------------------------</p><p>HINT: legit just think the opposite of</p>
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right handed alpha helix (B-form DNA)

spins counter-clockwise and is the most common structure

<p>spins counter-clockwise and is the most common structure</p>
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minor groove

A smaller groove that spirals around the DNA double helix.

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FUNCTION:

- provides a location where a protein can bind to a particular sequence of bases and affect gene expression

<p>A smaller groove that spirals around the DNA double helix.</p><p>--------------------------------</p><p>FUNCTION:</p><p>- provides a location where a protein can bind to a particular sequence of bases and affect gene expression</p>
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major groove

a larger groove that spirals around the DNA double helix

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FUNCTION:

- provides a location where a protein can bind to a particular sequence of bases and affect gene expression

<p>a larger groove that spirals around the DNA double helix</p><p>--------------------------------</p><p>FUNCTION:</p><p>- provides a location where a protein can bind to a particular sequence of bases and affect gene expression</p>
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Z-form DNA

- dsDNA

- left-handed alpha helix

- 12 base pairs per turn

- contains NO major or minor groove

- in vitro vs in vivo sides

- alters purine/pyrimidine sequences

- plays a role in transcription and chromosome structure

<p>- dsDNA </p><p>- left-handed alpha helix </p><p>- 12 base pairs per turn </p><p>- contains NO major or minor groove </p><p>- in vitro vs in vivo sides</p><p>- alters purine/pyrimidine sequences </p><p>- plays a role in transcription and chromosome structure</p>
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left handed alpha helix (Z-form DNA)

spins clockwise

<p>spins clockwise</p>
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in vitro vs in vivo sides

in vitro = outside a living cell

in vivo = inside a living cell

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in vitro the Z DNA has a high salt condition (meaning it has a higher ionic strength) than in vivo

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altering purine/pyrimidine sequences

the DNA strand continuously alternates between G and C due to high salt contractions

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EXAMPLE:

GCGCGCGCGCGC........

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transcription and chromosome structure

Z. Form DNA is responsible for mRNA to be formed

- it can be recognized by cellular proteins

- can alter chromosome compaction

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B vs Z DNA structure

B. DNA

- bases are perpendicular to the central axis (90 degrees)

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Z. DNA

- bases substantially tilted relative to central axis

- sugar-phosphate backbone has a zigzag pattern

<p>B. DNA</p><p>- bases are perpendicular to the central axis (90 degrees)</p><p>--------------------------------</p><p>Z. DNA</p><p>- bases substantially tilted relative to central axis</p><p>- sugar-phosphate backbone has a zigzag pattern</p>
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DNA structure

double-stranded structure stabilized by:

- hydrogen bonding between complementary bases

- Base stacking

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FEATURES:

- antiparallel

- contain 2 asymmetrical grooves on the outside of the helix (major and minor)

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RECAP:

DNA uses thymine as a base

DNA uses deoxyribose with 2' H

<p>double-stranded structure stabilized by: </p><p>- hydrogen bonding between complementary bases</p><p>- Base stacking </p><p>--------------------------------</p><p>FEATURES: </p><p>- antiparallel </p><p>- contain 2 asymmetrical grooves on the outside of the helix (major and minor) </p><p>--------------------------------</p><p>RECAP: </p><p>DNA uses thymine as a base </p><p>DNA uses deoxyribose with 2' H </p>
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Hydrogen bonding between complementary bases

A-T = 2 hydrogen bonds

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C-G= 3 hydrogen bonds

<p>A-T = 2 hydrogen bonds</p><p>--------------------------------</p><p>C-G= 3 hydrogen bonds</p>
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base stacking

bases are oriented so that the flattened regions are facing each other

<p>bases are oriented so that the flattened regions are facing each other</p>
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triple helix (OREO)

HISTORY:

founded by Alexander Rich by forming DNA pieces that were made synthetically to synthesize the base structure

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SEQUENCE:

- T binds to AT pair in biological DNA

- C binds to CG pair in biological DNA

<p>HISTORY:</p><p>founded by Alexander Rich by forming DNA pieces that were made synthetically to synthesize the base structure</p><p>--------------------------------</p><p>SEQUENCE:</p><p>- T binds to AT pair in biological DNA</p><p>- C binds to CG pair in biological DNA</p>
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RNA structure

- "are usually" single-stranded

- are typically several hundred to thousand nucleotides in length

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RECAP:

- RNA uses Uracil as a base

- RNA uses Ribose with 2' OH

<p>- "are usually" single-stranded</p><p>- are typically several hundred to thousand nucleotides in length</p><p>--------------------------------</p><p>RECAP:</p><p>- RNA uses Uracil as a base</p><p>- RNA uses Ribose with 2' OH</p>
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RNA synthesis

only one of the two strands of DNA is used as a template

<p>only one of the two strands of DNA is used as a template</p>
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why is RNA bad in alkaline solutions?

the bases can easily deprotonate the hydrogen from the hydroxyl group on the 2'-carbon atom

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RNA base pairings rules

Secondary stucture if formed due to complementary base pairing.

A-U

C-G

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- allows for short regions to form a double helix

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RNA double helices

is very uncommon

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FEATURES:

- are right-handed alpha helixes

- have the A form with 11 to 12 base pairs in turn

<p>is very uncommon</p><p>--------------------------------</p><p>FEATURES:</p><p>- are right-handed alpha helixes</p><p>- have the A form with 11 to 12 base pairs in turn</p>
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RNA secondary structures

The structures themselves are formed as signals to recruit/attract proteins

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TYPES OF STRUCTURES:

- Bulge loop

- Internal Loop

- Multibranched Loop

- Stem Loop

<p>The structures themselves are formed as signals to recruit/attract proteins </p><p>--------------------------------</p><p>TYPES OF STRUCTURES: </p><p>- Bulge loop</p><p>- Internal Loop</p><p>- Multibranched Loop</p><p>- Stem Loop</p>
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bulge loop

similar to stem-loop but no stem

<p>similar to stem-loop but no stem</p>
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internal loop

unpaired nucleotides on either side of the stem

- contains a loop with no pairings

<p>unpaired nucleotides on either side of the stem</p><p>- contains a loop with no pairings</p>
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Multibranched Loop

Crossed nucleotides

<p>Crossed nucleotides</p>
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Stem loop RNA

strand folds back on itself

- contains a loop with no pairings

- contains a stem unlike a Bulge loop

- stem contains base pairs

<p>strand folds back on itself</p><p>- contains a loop with no pairings </p><p>- contains a stem unlike a Bulge loop</p><p>- stem contains base pairs</p>
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template strand

The DNA strand that provides the template for ordering the sequence of nucleotides in an mRNA transcript.

<p>The DNA strand that provides the template for ordering the sequence of nucleotides in an mRNA transcript.</p>
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non-template strand (coding strand)

the strand of DNA that is not transcribed into RNA during transcription

<p>the strand of DNA that is not transcribed into RNA during transcription</p>